Pierret Chris, Morrison Jason A, Kirk Mark D
Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA.
Acta Neurobiol Exp (Wars). 2008;68(3):429-42. doi: 10.55782/ane-2008-1709.
Recent advances in our understanding of lysosomal storage disorders (LSDs) may lead to new therapies to treat the neuronal ceroid-lipofuscinoses (NCLs). In this review, enzyme replacement therapy, gene therapy, cell-mediated therapy and pharmaceutical treatments are considered across the LSDs and extended to therapies for the NCLs. It is likely that a combination of approaches will produce the most beneficial clinical outcome for treatment of pathologies displayed by the NCLs.
我们对溶酶体贮积症(LSDs)认识的最新进展可能会带来治疗神经元蜡样脂褐质沉积症(NCLs)的新疗法。在本综述中,我们讨论了针对溶酶体贮积症的酶替代疗法、基因疗法、细胞介导疗法和药物治疗,并将其扩展至针对神经元蜡样脂褐质沉积症的疗法。多种方法联合使用可能会为治疗神经元蜡样脂褐质沉积症所表现出的病症带来最有益的临床效果。